Histopathological insights into treatment failure with the levonorgestrel releasing intrauterine system in women with heavy menstrual bleeding: a retrospective study

In: International Journal of Reproduction, Contraception, Obstetrics and Gynecology · 2026 · vol. 15(2) , pp. 579–582 · doi:10.18203/2320-1770.ijrcog20260178 · W7126079714
article OA: diamond CC0
AI-generated summary by claude@2026-06, 2026-06-08

This retrospective study of 88 women found that levonorgestrel-releasing intrauterine system treatment failure for heavy menstrual bleeding was primarily associated with underlying uterine pathologies, especially adenomyosis.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-09 · read from full text

This retrospective study (BARC Hospital, Mumbai; Jan 2017–Mar 2020) evaluated 88 women with heavy menstrual bleeding treated with a levonorgestrel-releasing intrauterine system (LNG-IUS), identifying non-responders as those with persistent heavy bleeding and examining endometrial biopsy and, in some cases, hysterectomy specimens for histopathological correlates of treatment failure. Treatment failure occurred in 26 women (29.5%), and among biopsy findings, proliferative endometrium (65.4%), disordered proliferative endometrium (19.2%), and secretory endometrium (15.4%) were reported. Of nine hysterectomy specimens from non-responders, adenomyosis was most frequent (44.4%), followed by adenomyosis with leiomyoma (33.3%), endometrial polyp (11.1%), and leiomyoma (11.1%). The paper’s major caveat is its retrospective design and small number of hysterectomy-provided histology samples for non-responders. This paper is centrally about endometriosis and/or adenomyosis—specifically adenomyosis associated with histopathological findings in LNG-IUS treatment failure for heavy menstrual bleeding.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Background: The levonorgestrel-releasing intrauterine system (LNG-IUS) is an established first-line therapy for heavy menstrual bleeding (HMB), effectively reducing menstrual blood loss and improving quality of life in most women. However, a subset of patients fails to achieve adequate response, warranting evaluation of potential underlying causes. Methods: This retrospective study was conducted at BARC Hospital, Mumbai, from January 2017 to March 2020, and included 88 women with HMB treated with LNG-IUS. Non-responders were identified based on persistent heavy bleeding despite therapy. Endometrial biopsy and, where applicable, hysterectomy specimens were analyzed to determine histopathological findings associated with treatment failure. Results: Of the 88 women treated, 26 (29.5%) were classified as non-responders. Endometrial biopsy revealed proliferative endometrium in 65.4%, disordered proliferative endometrium in 19.2%, and secretory endometrium in 15.4% of cases. Among nine non-responders who underwent hysterectomy, adenomyosis was the most common finding (44.4%), followed by adenomyosis with leiomyoma (33.3%), endometrial polyp (11.1%), and leiomyoma (11.1%). Conclusions: Treatment failure of LNG-IUS in women with HMB was predominantly associated with structural uterine abnormalities, particularly adenomyosis. Comprehensive pre-insertion evaluation, including clinical and imaging assessment, is essential to detect underlying pathology and optimize patient selection. Individualized management based on uterine morphology and symptom profile may improve therapeutic success and reduce delays in achieving symptom control.
Full text 4,937 characters · extracted from oa-doi-fallback · 5 sections · click to expand

Background

The levonorgestrel-releasing intrauterine system (LNG-IUS) is an established first-line therapy for heavy menstrual bleeding (HMB), effectively reducing menstrual blood loss and improving quality of life in most women. However, a subset of patients fails to achieve adequate response, warranting evaluation of potential underlying causes.

Methods

This retrospective study was conducted at BARC Hospital, Mumbai, from January 2017 to March 2020, and included 88 women with HMB treated with LNG-IUS. Non-responders were identified based on persistent heavy bleeding despite therapy. Endometrial biopsy and, where applicable, hysterectomy specimens were analyzed to determine histopathological findings associated with treatment failure.

Results

Of the 88 women treated, 26 (29.5%) were classified as non-responders. Endometrial biopsy revealed proliferative endometrium in 65.4%, disordered proliferative endometrium in 19.2%, and secretory endometrium in 15.4% of cases. Among nine non-responders who underwent hysterectomy, adenomyosis was the most common finding (44.4%), followed by adenomyosis with leiomyoma (33.3%), endometrial polyp (11.1%), and leiomyoma (11.1%).

Conclusions

Treatment failure of LNG-IUS in women with HMB was predominantly associated with structural uterine abnormalities, particularly adenomyosis. Comprehensive pre-insertion evaluation, including clinical and imaging assessment, is essential to detect underlying pathology and optimize patient selection. Individualized management based on uterine morphology and symptom profile may improve therapeutic success and reduce delays in achieving symptom control. Metrics

References

Munro MG, Critchley HOD, Fraser IS. The FIGO classification of causes of abnormal uterine bleeding in the reproductive years. Int J Gynaecol Obstet. 2011;113(1):3-13. DOI: https://doi.org/10.1016/j.ijgo.2010.11.011 Nidhi, Kumari A, Tirkey S, Prakash J. Effectiveness of levonorgestrel-releasing intrauterine system in perimenopausal women with heavy menstrual bleeding: a prospective study at a teaching hospital in India. J Menopausal Med. 2022;28(3):128-35. DOI: https://doi.org/10.6118/jmm.22025 Chen S, Liu J, Peng S, Zheng Y. Levonorgestrel intrauterine system versus medical therapy for heavy menstrual bleeding: A systematic review and meta-analysis. Front Med. 2022;9:948709. DOI: https://doi.org/10.3389/fmed.2022.948709 Struble J, Reid S, Bedaiwy MA. Adenomyosis: a clinical review of a challenging gynecologic condition. J Minim Invasive Gynecol. 2016;23(2):164-85. DOI: https://doi.org/10.1016/j.jmig.2015.09.018 Lethaby A, Hussain M, Rishworth JR, Rees MC. Progesterone or progestogen-releasing intrauterine systems for heavy menstrual bleeding. Cochrane Database Syst Rev. 2015;30(4):CD002126. DOI: https://doi.org/10.1002/14651858.CD002126.pub3 Wildemeersch D, Janssens D, Andrade A. Management of heavy menstrual bleeding in the community: long-term efficacy of the levonorgestrel-releasing intrauterine system. Eur J Contracept Reprod Health Care. 2018;23(3):206-12. Xiao B, Wu SC, Chong J, Zeng T, Han LH, Luukkainen T. Therapeutic effects of the levonorgestrel-releasing intrauterine system in the treatment of idiopathic menorrhagia. Fertil Steril. 2003;79(4):963-9. DOI: https://doi.org/10.1016/S0015-0282(02)04913-0 Wiebe E, Trussell J. Discontinuation rates and acceptability during 1 year of using the levonorgestrel intrauterine ball. Contraception. 2016;93(4):364-6. DOI: https://doi.org/10.1016/j.contraception.2015.12.002 Kriplani A, Singh BM, Lal S, Agarwal N. Efficacy and safety of the levonorgestrel intrauterine system (LNG-IUS) in menorrhagia: a pilot study from India. Int J Gynaecol Obstet. 2007;97(3):190-4. DOI: https://doi.org/10.1016/j.ijgo.2007.01.009 Taran FA, Wallwiener M, Kabashi D, Rothmund R, Rall K, Kraemer B, et al. Clinical characteristics indicating adenomyosis at the time of hysterectomy: a retrospective analysis. Arch Gynecol Obstet. 2012;285(6):1571-6. DOI: https://doi.org/10.1007/s00404-011-2180-7 Vercellini P, Consonni D, Dridi D, Bracco B, Frattaruolo MP, Somigliana E. Uterine adenomyosis and in vitro fertilization outcome: a systematic review and meta-analysis. Hum Reprod. 2014;29(5):964-77. DOI: https://doi.org/10.1093/humrep/deu041 Shaaban OM, Ali MK, Sabra AM, Abd El Aal DE. Levonorgestrel-releasing intrauterine system versus a low-dose combined oral contraceptive for treatment of adenomyotic uteri: a randomized clinical trial. Contraception. 2015;92(4):301-7. DOI: https://doi.org/10.1016/j.contraception.2015.05.015

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

adenomyosis

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (11)

Source provenance

openalex
last seen: 2026-06-04T00:00:01.174412+00:00
License: CC0 · commercial use OK